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DNA methylation of the filaggrin gene adds to the risk of eczema associated with loss‐of‐function variants

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Position of a ‘green–red’ hybrid gene in the visual pigment array determines colour-vision phenotype

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APOE polymorphism and its effect on plasma C-reactive protein levels in a large general population sample

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C-Reactive Protein Genotypes Affect Baseline, but not Exercise Training–Induced Changes, in C-Reactive Protein Levels

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Interleukin-8 promoter polymorphism -251A/T is a risk factor for age-related macular degeneration

Goverdhan, S. V., Ennis, S., Hannan, S. R., Madhusudhana, K. C., Cree, A. J., Luff, A. J., & Lotery, A. J. (2008) · British Journal of Ophthalmology · doi:10.1136/bjo.2007.123190 · Cited by 79

Functional polymorphism of the matrix metalloproteinase-9 (MMP-9) gene in schizophrenia.

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Association of HLA Class I and Class II Polymorphisms with Age-Related Macular Degeneration

Goverdhan, S. V., Howell, M. W., Mullins, R. F., Osmond, C., Hodgkins, P. R., Self, J., Avery, K., & Lotery, A. J. (2005) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.04-0928 · Cited by 78

High-Resolution Homozygosity Mapping Is a Powerful Tool to Detect Novel Mutations Causative of Autosomal Recessive RP in the Dutch Population

Collin, R. W. J., van den Born, L. I., Klevering, B. J., de Castro-Miró, M., Littink, K. W., Arimadyo, K., Azam, M., Yazar, V., Zonneveld, M. N., Paun, C. C., et al. (2011) · Investigative Opthalmology & Visual Science · doi:10.1167/iovs.10-6185 · Cited by 79

Longitudinal multi-level biomarker analysis of BDNF in major depression and bipolar disorder

Schröter, K., Brum, M., Brunkhorst-Kanaan, N., Tole, F., Ziegler, C., Domschke, K., Reif, A., & Kittel-Schneider, S. (2020) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-019-01007-y · Cited by 68

Symptoms in carriers of adrenoleukodystrophy relate to skewed X inactivation

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Characterization of a New Form of Inherited Hypercholesterolemia: Familial Recessive Hypercholesterolemia

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Plasma proteins, cognitive decline, and 20-year risk of dementia in the Whitehall II and Atherosclerosis Risk in Communities studies

Lindbohm, J. V., Mars, N., Walker, K. A., Singh‐Manoux, A., Livingston, G., Brunner, E. J., Sipilä, P. N., Saksela, K., Ferrie, J. E., Lovering, R. C., et al. (2022) · Alzheimer's & Dementia · doi:10.1002/alz.12419 · Cited by 70

Natural gene therapy in monozygotic twins with Fanconi anemia

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Severe oxidatively damaged DNA after cisplatin treatment of cancer patients

Siomek, A., Tujakowski, J., Gackowski, D., Rozalski, R., Foksinski, M., Dziaman, T., Roszkowski, K., & Olinski, R. (2006) · International Journal of Cancer · doi:10.1002/ijc.22088 · Cited by 67

Evaluation of tumor necrosis factor (TNF)-α mRNA expression level and the rs1799964 polymorphism of the TNF-α gene in peripheral mononuclear cells of patients with inflammatory bowel diseases

Nourian, M., Chaleshi, V., Pishkar, L., Azimzadeh, P., Baradaran Ghavami, S., Balaii, H., Alinaghi, S., Shahrokh, S., Asadzadeh Aghdaei, H., & Zali, M. R. (2017) · Biomedical Reports · doi:10.3892/br.2017.908 · Cited by 66

Effects of chronic interpersonal stress exposure on depressive symptoms are moderated by genetic variation at IL6 and IL1β in youth

Tartter, M., Hammen, C., Bower, J. E., Brennan, P. A., & Cole, S. (2015) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2015.01.003 · Cited by 66

MAOA promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in indian children

Das, M., Das Bhowmik, A., Sinha, S., Chattopadhyay, A., Chaudhuri, K., Singh, M., & Mukhopadhyay, K. (2006) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30385 · Cited by 63

Longer telomere length in patients with schizophrenia

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Glucocorticoid receptor gene methylation and HPA-axis regulation in adolescents. The TRAILS study

van der Knaap, L. J., Oldehinkel, A. J., Verhulst, F. C., van Oort, F. V. A., & Riese, H. (2015) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2015.04.012 · Cited by 60

Genotype-phenotype associations in non-classical steroid 21-hydroxylase deficiency

Weintrob, N., Brautbar, C., Pertzelan, A., Josefsberg, Z., Dickerman, Z., Kauschansky, A., Lilos, P., Peled, D., Phillip, M., & Israel, S. (2000) · European Journal of Endocrinology · doi:10.1530/eje.0.1430397 · Cited by 59

Perinatal risk factors interacting with catechol O‐methyltransferase and the serotonin transporter gene predict ASD symptoms in children with ADHD

Nijmeijer, J. S., Hartman, C. A., Rommelse, N. N. J., Altink, M. E., Buschgens, C. J. M., Fliers, E. A., Franke, B., Minderaa, R. B., Ormel, J., Sergeant, J. A., et al. (2010) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2010.02277.x · Cited by 57

Reduced telomere length in neurodegenerative disorders may suggest shared biology

Kota, L. N., Bharath, S., Purushottam, M., Moily, N. S., Sivakumar, P. T., Varghese, M., Pal, P. K., & Jain, S. (2015) · The Journal of Neuropsychiatry and Clinical Neurosciences · doi:10.1176/appi.neuropsych.13100240 · Cited by 53

Telomere fusions in early human breast carcinoma

Tanaka, H., Abe, S., Huda, N., Tu, L., Beam, M. J., Grimes, B., & Gilley, D. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120062109 · Cited by 52

The BDNF Val66Met polymorphism is an independent risk factor for high lethality in suicide attempts of depressed patients

Schenkel, L. C., Segal, J., Becker, J. A., Manfro, G. G., Bianchin, M. M., & Leistner-Segal, S. (2010) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2010.04.023 · Cited by 53

Human N-acetyltransferase 1 *10 and *11 alleles increase protein expression through distinct mechanisms and associate with sulfamethoxazole-induced hypersensitivity

Wang, D., Para, M. F., Koletar, S. L., & Sadee, W. (2011) · Pharmacogenetics and Genomics · doi:10.1097/fpc.0b013e3283498ee9 · Cited by 53

A new de novo Notch3 mutation causing CADASIL

Coto, E., Menéndez, M., Navarro, R., García‐Castro, M., & Alvarez, V. (2006) · European Journal of Neurology · doi:10.1111/j.1468-1331.2006.01337.x · Cited by 51

Association analysis of the dopamine D2receptor gene in Tourette's syndrome using the haplotype relative risk method

Nöthen, M. M., Hebebrand, J., Knapp, M., Hebebrand, K., Camps, A., von Gontard, A., Wettke‐Schäfer, R., Lisch, S., Cichon, S., Poustka, F., et al. (1994) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320540311 · Cited by 52

Differential reproductive efficiency associated with common apolipoprotein E alleles in postreproductive-aged subjects

Corbo, R. M., Scacchi, R., & Cresta, M. (2004) · Fertility and Sterility · doi:10.1016/j.fertnstert.2003.05.029 · Cited by 52

Thr92Ala polymorphism in the type 2 deiodinase is not associated with T4 dose in athyroid patients or patients with Hashimoto thyroiditis

Heemstra, K. A., Hoftijzer, H. C., Van Der Deure, W. M., Peeters, R. P., Fliers, E., Appelhof, B. C., Wiersinga, W. M., Corssmit, E. P. M., Visser, T. J., & Smit, J. W. A. (2009) · Clinical Endocrinology · doi:10.1111/j.1365-2265.2008.03474.x · Cited by 51

Fatigue and fatigue-related symptoms in patients treated for different causes of hypothyroidism

Louwerens, M., Appelhof, B. C., Verloop, H., Medici, M., Peeters, R. P., Visser, T. J., Boelen, A., Fliers, E., Smit, J. W. A., & Dekkers, O. M. (2012) · European Journal of Endocrinology · doi:10.1530/eje-12-0501 · Cited by 50

Genetic deficiency of complement factor H in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis

Montes, T., Goicoechea de Jorge, E., Ramos, R., Gomà, M., Pujol, O., Sánchez-Corral, P., & Rodríguez de Córdoba, S. (2008) · Molecular Immunology · doi:10.1016/j.molimm.2008.01.027 · Cited by 47

Age-related Macular Degeneration and Modification of Systemic Complement Factor H Production Through Liver Transplantation

Khandhadia, S., Hakobyan, S., Heng, L. Z., Gibson, J., Adams, D. H., Alexander, G. J., Gibson, J. M., Martin, K. R., Menon, G., Nash, K., et al. (2013) · Ophthalmology · doi:10.1016/j.ophtha.2013.01.004 · Cited by 47

The cardiovascular and hypothalamus-pituitary-adrenal axis response to stress is controlled by glucocorticoid receptor sequence variants and promoter methylation

Li-Tempel, T., Larra, M. F., Sandt, E., Mériaux, S. B., Schote, A. B., Schächinger, H., Muller, C. P., & Turner, J. D. (2016) · Clinical Epigenetics · doi:10.1186/s13148-016-0180-y · Cited by 46

Genetic evidence for the Mongolian ancestry of Kalmyks

Nasidze, I., Quinque, D., Dupanloup, I., Cordaux, R., Kokshunova, L., & Stoneking, M. (2005) · American Journal of Physical Anthropology · doi:10.1002/ajpa.20159 · Cited by 46

Folate and long-chain polyunsaturated fatty acid supplementation during pregnancy has long-term effects on the attention system of 8.5-y-old offspring: a randomized controlled trial

Catena, A., Muñoz-Machicao, J. A., Torres-Espínola, F. J., Martínez-Zaldívar, C., Diaz-Piedra, C., Gil, A., Haile, G., Györei, E., Molloy, A. M., Decsi, T., et al. (2016) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.115.109108 · Cited by 46

Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant

Pálmason, H., Moser, D., Sigmund, J., Vogler, C., Hänig, S., Schneider, A., Seitz, C., Marcus, A., Meyer, J., & Freitag, C. M. (2010) · Journal of Neural Transmission · doi:10.1007/s00702-009-0338-2 · Cited by 44

Mutations in CYP11B1 and congenital adrenal hyperplasia in Moroccan Jews

Paperna, T., Gershoni-Baruch, R., Badarneh, K., Kasinetz, L., & Hochberg, Z. (2005) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2005-1145 · Cited by 43

The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene

Rocha, R. O., Billerbeck, A. E. C., Pinto, E. M., Melo, K. F. S., Lin, C. J., Longui, C. A., Mendonca, B. B., & Bachega, T. A. S. S. (2008) · Clinical Endocrinology · doi:10.1111/j.1365-2265.2007.03023.x · Cited by 43

Applicability of the IAIHG scoring system to the diagnosis of antimitochondrial/anti‐M2 seropositive variant form of autoimmune hepatitis

Farias, A. Q., Gonçalves, L. L., Bittencourt, P. L., De Melo, E. S., Abrantes‐Lemos, C. P., Porta, G., Nakhle, M. C., Carrilho, F. J., & Cancado, E. L. R. (2006) · Journal of Gastroenterology and Hepatology · doi:10.1111/j.1440-1746.2006.04130.x · Cited by 43

Endometrial vezatin and its association with endometriosis risk

Holdsworth-Carson, S. J., Fung, J. N., Luong, H. T. T., Sapkota, Y., Bowdler, L. M., Wallace, L., Teh, W. T., Powell, J. E., Girling, J. E., Healey, M., et al. (2016) · Human Reproduction · doi:10.1093/humrep/dew047 · Cited by 41

Tumor necrosis factor SNP haplotypes are associated with iron deficiency anemia in West African children

Atkinson, S. H., Rockett, K. A., Morgan, G., Bejon, P. A., Sirugo, G., O'Connell, M. A., Hanchard, N., Kwiatkowski, D. P., & Prentice, A. M. (2008) · Blood · doi:10.1182/blood-2008-06-162008 · Cited by 43

Epigenetic Response to Mindfulness in Peripheral Blood Leukocytes Involves Genes Linked to Common Human Diseases

García-Campayo, J., Puebla-Guedea, M., Labarga, A., Urdánoz, A., Roldán, M., Pulido, L., de Morentin, X. M., Perdones-Montero, Á., Montero-Marín, J., & Mendioroz, M. (2018) · Mindfulness · doi:10.1007/s12671-017-0851-6 · Cited by 42

Low Intake of Vitamin E Accelerates Cellular Aging in Patients With Established Cardiovascular Disease: The CORDIOPREV Study

Corina, A., Rangel-Zúñiga, O. A., Jiménez-Lucena, R., Alcalá-Díaz, J. F., Quintana-Navarro, G., Yubero-Serrano, E. M., López-Moreno, J., Delgado-Lista, J., Tinahones, F., Ordovás, J. M., et al. (2019) · The Journals of Gerontology: Series A · doi:10.1093/gerona/gly195 · Cited by 41

Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche

Ghizzoni, L., Cappa, M., Vottero, A., Ubertini, G., Carta, D., Di Iorgi, N., Gasco, V., Marchesi, M., Raggi, V., Ibba, A., et al. (2011) · European Journal of Endocrinology · doi:10.1530/eje-11-0119 · Cited by 41

Early-Onset Foveal Involvement in Retinitis Punctata Albescens With Mutations in RLBP1

Dessalces, E., Bocquet, B., Bourien, J., Zanlonghi, X., Verdet, R., Meunier, I., & Hamel, C. P. (2013) · JAMA Ophthalmology · doi:10.1001/jamaophthalmol.2013.4476 · Cited by 41

Rare TLR2 mutations reduce TLR2 receptor function and can increase atopy risk

Kormann, M. S. D., Ferstl, R., Depner, M., Klopp, N., Spiller, S., Illig, T., Vogelberg, C., Von Mutius, E., Kirschning, C. J., & Kabesch, M. (2009) · Allergy · doi:10.1111/j.1398-9995.2008.01891.x · Cited by 39

Catechol‐O‐methyltransferase gene methylation and substance use in adolescents: the TRAILS study

van der Knaap, L. J., Schaefer, J. M., Franken, I. H. A., Verhulst, F. C., van Oort, F. V. A., & Riese, H. (2014) · Genes, Brain and Behavior · doi:10.1111/gbb.12147 · Cited by 38

Composition and maternal origin of the neonatal oral cavity microbiota

Tuominen, H., Collado, M. C., Rautava, J., Syrjänen, S., & Rautava, S. (2019) · Journal of Oral Microbiology · doi:10.1080/20002297.2019.1663084 · Cited by 39

Interaction between CRHR1 and BDNF genes increases the risk of recurrent major depressive disorder in Chinese population

Xiao, Z., Liu, W., Gao, K., Wan, Q., Yang, C., Wang, H., Wang, X., Wang, G., & Liu, Z. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028733 · Cited by 37

Common variants of human TERT and TERC genes and susceptibility to sporadic Alzheimers disease

Scarabino, D., Broggio, E., Gambina, G., Pelliccia, F., & Corbo, R. M. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2016.12.017 · Cited by 36

Genetic variants in nuclear-encoded mitochondrial proteins are associated with oxidative stress in obsessive compulsive disorders

Orhan, N., Kucukali, C. I., Cakir, U., Seker, N., & Aydin, M. (2012) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2011.09.012 · Cited by 36

Association between the brain-derived neurotrophic factor Val66Met polymorphism and therapeutic response to olanzapine in schizophrenia patients

Nikolac Perkovic, M., Nedic Erjavec, G., Zivkovic, M., Sagud, M., Uzun, S., Mihaljevic-Peles, A., Kozumplik, O., Muck-Seler, D., & Pivac, N. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3515-4 · Cited by 35

Neurological impairment among heterozygote women for X-linked Adrenoleukodystrophy: a case control study on a clinical, neurophysiological and biochemical characteristics

Habekost, C. T., Schestatsky, P., Torres, V. F., de Coelho, D. M., Vargas, C. R., Torrez, V., Oses, J. P., Portela, L. V., Pereira, F. D. S., Matte, U., et al. (2014) · Orphanet Journal of Rare Diseases · doi:10.1186/1750-1172-9-6 · Cited by 35

The OXTR Single-Nucleotide Polymorphism rs53576 Moderates the Impact of Childhood Maltreatment on Empathy for Social Pain in Female Participants: Evidence for Differential Susceptibility

Flasbeck, V., Moser, D., Kumsta, R., & Brüne, M. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00359 · Cited by 34

Spondyloepimetaphyseal dysplasia with joint laxity (Beighton type); mutation analysis in eight affected South African families

Vorster, A. A., Beighton, P., & Ramesar, R. S. (2015) · Clinical Genetics · doi:10.1111/cge.12413 · Cited by 34

Apolipoprotein E1-Hammersmith (Lys146 → Asn;Arg147 → Trp), due to a dinucleotide substitution, is associated with early manifestation of dominant type III hyperlipoproteinaemia

Hoffer, M. J. V., Niththyananthan, S., Naoumova, R. P., Kibirige, M. S., Frants, R. R., Havekes, L. M., & Thompson, G. R. (1996) · Atherosclerosis · doi:10.1016/0021-9150(96)05819-4 · Cited by 32

Mutations, Clinical Findings and Survival Estimates in South American Patients with X-Linked Adrenoleukodystrophy

Pereira, F. D. S., Matte, U., Habekost, C. T., Castilhos, R. M. D., El Husny, A. S., Lourenço, C. M., Vianna-Morgante, A. M., Giuliani, L., Galera, M. F., Honjo, R., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034195 · Cited by 30

Glycohemoglobin results in samples with hemoglobin C or S trait: a comparison of four test systems

Roberts, W. L., Chiasera, J. M., & Ward-Cook, K. M. (1999) · Clinical Chemistry · doi:10.1093/clinchem/45.6.906 · Cited by 28

Intraspecific variation in mitochondrial DNA of muskoxen, based on control-region sequences

Groves, P. (1997) · Canadian Journal of Zoology · doi:10.1139/z97-070 · Cited by 27

Low genetic variation in muskoxen (Ovibos moschatus) from western Greenland using microsatellites

Holm, L. ‐., Forchhammer, M. C., & Boomsma, J. J. (1999) · Molecular Ecology · doi:10.1046/j.1365-294x.1999.00615.x · Cited by 26

A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder

Dadkhah, T., Rahimi-Aliabadi, S., Jamshidi, J., Ghaedi, H., Taghavi, S., Shokraeian, P., Akhavan-Niaki, H., Tafakhori, A., Ohadi, M., & Darvish, H. (2017) · Journal of Affective Disorders · doi:10.1016/j.jad.2016.10.008 · Cited by 26

MtDNA and Y-chromosome variation in Kurdish groups.

Nasidze, I., Quinque, D., Ozturk, M., Bendukidze, N., & Stoneking, M. (2005) · Annals of Human Genetics · doi:10.1046/j.1529-8817.2005.00174.x · Cited by 26

TWGDAM Validation of a Nine-Locus and a Four-Locus Fluorescent STR Multiplex System

Micka, K., Amiott, E., Hockenberry, T., Sprecher, C., Lins, A., Rabbach, D., Taylor, J., Bacher, J., Glidewell, D., Gibson, S., et al. (1999) · Journal of Forensic Sciences · doi:10.1520/jfs14595j · Cited by 25

Association between vaspin rs2236242 gene polymorphism and polycystic ovary syndrome risk

Kohan, L., Zarei, A., Fallahi, S., & Tabiee, O. (2014) · Gene · doi:10.1016/j.gene.2014.01.078 · Cited by 23

LRP‐associated protein gene (LRPAP1) and susceptibility to degenerative dementia

Pandey, P., Pradhan, S., & Mittal, B. (2008) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2008.00436.x · Cited by 23

Lack of association between the HLA-DRB1 locus and post-streptococcal reactive arthritis and acute rheumatic fever in italian children

Simonini, G., Porfirio, B., Cimaz, R., Calabri, G. B., Giani, T., & Falcini, F. (2004) · Seminars in Arthritis and Rheumatism · doi:10.1016/j.semarthrit.2004.04.001 · Cited by 22

Relationship between plasma HDL subclasses distribution and lipoprotein lipase gene HindIII polymorphism in hyperlipidemia

Long, S., Tian, Y., Zhang, R., Yang, L., Xu, Y., Jia, L., & Fu, M. (2006) · Clinica Chimica Acta · doi:10.1016/j.cca.2005.11.010 · Cited by 21

Interactions Among Polymorphisms of Susceptibility Loci for Alzheimer’s Disease or Depressive Disorder

Kitzlerová, E., Fišar, Z., Lelková, P., Jirák, R., Zvěřová, M., Hroudová, J., Manukyan, A., Martásek, P., & Raboch, J. (2018) · Medical Science Monitor · doi:10.12659/msm.907202 · Cited by 21

The Presence of Telomere Fusion in Sporadic Colon Cancer Independently of Disease Stage, TP53/KRAS Mutation Status, Mean Telomere Length, and Telomerase Activity

Tanaka, H., Beam, M. J., & Caruana, K. (2014) · Neoplasia · doi:10.1016/j.neo.2014.08.009 · Cited by 19

Association of Plasma Aβ40 Peptides, But Not Aβ42, with Coronary Artery Disease and Diabetes Mellitus

Roeben, B., the TREND study team, Maetzler, W., Vanmechelen, E., Schulte, C., Heinzel, S., Stellos, K., Godau, J., Huber, H., Brockmann, K., et al. (2016) · Journal of Alzheimer's Disease · doi:10.3233/jad-150575 · Cited by 19

Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: characterization of three novel polymorphisms

Ben Charfeddine, I., Riepe, F. G., Clauser, E., Ayedi, A., Makni, S., Sfar, M. T., Sboui, H., Kahloul, N., Ben Hamouda, H., Chouchane, S., et al. (2012) · Gene · doi:10.1016/j.gene.2012.07.027 · Cited by 19

Serotonin 5-HT2A receptor polymorphisms are associated with irritability and aggression in conduct disorder

Nedic Erjavec, G., Tudor, L., Nikolac Perkovic, M., Podobnik, J., Dodig Curkovic, K., Curkovic, M., Svob Strac, D., Cusek, M., Bortolato, M., & Pivac, N. (2022) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2022.110542 · Cited by 18

Next‐generation sequencing targeted disease panel in rod‐cone retinal dystrophies in Māori and Polynesian reveals novel changes and a common founder mutation

Vincent, A. L., Abeysekera, N., van Bysterveldt, K. A., Oliver, V. F., Ellingford, J. M., Barton, S., & Black, G. C. (2017) · Clinical & Experimental Ophthalmology · doi:10.1111/ceo.12983 · Cited by 18

Intragenic probe used for diagnostics in fragile X families

Verkerk, A. J. M. H., De Vries, B. B. A., Niermeijer, M. F., Fu, Y., Nelson, D. L., Warren, S. T., Majoor‐Krakauer, D. F., Halley, D. J. J., & Oostra, B. A. (1992) · American Journal of Medical Genetics · doi:10.1002/ajmg.1320430132 · Cited by 17

A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epithelium

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Association, Haplotype, and Gene‐Gene Interactions of the HPA Axis Genes with Suicidal Behaviour in Affective Disorders

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